ERAS in Video-assisted Mediastinal Surgery

Fudan University

Status and phase: Unknown; Phase 1

Conditions: Enhanced Recovery After Surgery

Treatments: Combination Product: Traditional measures; Combination Product: ERAS

Study type: Interventional

Funder types: Other

Identifiers

NCT03271606

zs2017822

Details and patient eligibility

About

This is a single center, randomized,single blind study to investigate the effectiveness of enhanced recovery regimen (ERAS) in patients undergoing Video-assisted Mediastinal Surgery. And we also going to compare the effectiveness of ERAS with that of traditional regimen in these patients.

Full description

Compare to traditional measures, the ERAS protocal mainly includes:Good preoperative visit, shorten the fast time, minimumal invasive surgery procedures, fewer opioids and early movements after surgery. These items have been successfully used in colon cancer surgery, and we thus plan to investigate the effectiveness of these measures in mediastinal surgery.

Enrollment: 100 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients elective mediastinal surgery;
• BMI 18-30 kg/m2.

Exclusion criteria

• Patient refuse;
• ASA≥3;
• Patients allergic to used anesthetics (propofol,rocuronium), patients with liver and/or kidney and/or mental dysfunction.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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100 participants in 2 patient groups

ERAS group

Experimental group

Description:

The patients in this group receive enhanced measures perioperatively

Treatment:

Combination Product: ERAS

Traditional group

Active Comparator group

Description:

The patients in this group receive traditional measures perioperatively

Treatment:

Combination Product: Traditional measures